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EC number: 284-974-4 | CAS number: 85005-41-0
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Water solubility
Administrative data
- Endpoint:
- water solubility
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 March 2016 to 12 July 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
Cross-referenceopen allclose all
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
Reference
- Endpoint:
- melting point/freezing point
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 March 2016 to 12 July 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.1 (Melting / Freezing Temperature)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 102 (Melting point / Melting Range)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- differential scanning calorimetry
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No. of test material: CBI
- Expiration date of the lot/batch: 02 February 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature, in the dark - Key result
- Melting / freezing pt.:
- > 31 - < 62 °C
- Remarks on result:
- other: The melting transition of the test item was considered to be softening over a broad range.
- Conclusions:
- The melting temperature of the test item has been determined to be over the range 31 to 62 °C (304 to 335 K).
- Executive summary:
The melting temperature of the test substance was determined as over the range 31 to 62 °C (304 to 335 K), by differential scanning calorimetry, designed to be compatible with Method A.1 Melting/Freezing Temperature of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 102 of the OECD Guidelines for Testing of Chemicals, 27 July 1995.
Thermal Event | Interpretation | Temperature (⁰C) | |
Determination 1 | Determination 2 | ||
Endotherm | Melting range | 31.46 to 62.13 | 31.50 to 62.27 |
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
Reference
- Endpoint:
- boiling point
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 March 2016 to 12 July 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.2 (Boiling Temperature)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 103 (Boiling Point)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- differential scanning calorimetry
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No. of test material: CBI
- Expiration date of the lot/batch: 02 February 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature, in the dark - Key result
- Boiling pt.:
- 128 °C
- Atm. press.:
- 101 kPa
- Decomposition:
- yes
- Remarks on result:
- other: After heating to 400 °C, the samples had lost approximately 100% of their original weight.
- Conclusions:
- The test item has been determined to decompose from approximately 222 °C (495 K) at 100 kPa. As the test item decomposed, no value for boiling temperature could be determined.
- Executive summary:
Decomposition from approximately 222 °C (495 K) at 100 kPa, by differential scanning calorimetry, designed to be compatible with Method A.2 Boiling Temperature of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 103 of the OECD Guidelines for Testing of Chemicals, 27 July 1995. As the test item decomposed, no value for boiling temperature could be determined.
Thermal Event | Interpretation | Temperature (⁰C) | |||
Endotherm | Approximate onset of decomposition |
Determination 1 | Determination 2 | Determination 3 | Determination 4 |
228.45 | 229.82 | 221.82 | 236.07 |
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
Reference
- Endpoint:
- relative density
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 March 2016 to 12 July 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.3 (Relative Density)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 109 (Density of Liquids and Solids)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- pycnometer method
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No. of test material: CBI
- Expiration date of the lot/batch: 03 February 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature in the dark - Key result
- Type:
- relative density
- Density:
- 0.968 other: unitless
- Temp.:
- 20 °C
- Conclusions:
- The density of the test item has been determined to be 968 kg/m3 at 20.0 ± 2.0 °C and a relative density of 0.968.
- Executive summary:
The test substance density was deteremined to be 968 kg/m3 at 20.0 ± 2.0 °C, relative density of 0.968, by gas comparison pycnometer,, designed to be compatible with Method A.3 Relative Density of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 109 of the OECD Guidelines for Testing of Chemicals, 02 October 2012.
Determination | Mean Volume of Vessel (cm3) |
Mean Volume of Vessel and Test Item (cm3) |
Volume of Test Item (cm3) | Density (kg/m3) |
1 | 14.1 | 55.9 | 41.9 | 968 |
2 | 14.4 | 59.8 | 45.4 | 967 |
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
Reference
- Endpoint:
- partition coefficient
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 March 2016 to 12 July 2016
- Reliability:
- 1 (reliable without restriction)
- Rationale for reliability incl. deficiencies:
- guideline study
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.8 (Partition Coefficient - Shake Flask Method)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 117 (Partition Coefficient (n-octanol / water), HPLC Method)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- HPLC method
- Partition coefficient type:
- octanol-water
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No. of test material: CBI
- Expiration date of the lot/batch: 02 February 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature, in the dark - Analytical method:
- high-performance liquid chromatography
- Key result
- Type:
- log Pow
- Partition coefficient:
- > 5.71
- Temp.:
- 20 °C
- pH:
- 5.9
- Details on results:
- Preliminary Estimate: The estimated log10 Pow for the representative structure of the test item was calculated to be from 5.71.
Definitive Test: The partition coefficient of the test item has been determined to be >1.0 x 1010 with a log10 Pow of >10.0. - Conclusions:
- The partition coefficient of the test item has been determined to be >1.0 x 10^10 with a log10 Pow of >10.0.
- Executive summary:
The partition coefficient (n-octanol/water) was determinded to be greater than 1.0 x 10^10, log10 Pow of >10.0, using the HPLC method, designed to be compatible with Method A.8 Partition Coefficient of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 117 of the OECD Guidelines for Testing of Chemicals, 13 April 2004.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
Reference
- Endpoint:
- surface tension
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 07 March 2016 to 12 July 2016
- Reliability:
- 1 (reliable without restriction)
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Reason / purpose for cross-reference:
- other: Study report pertains to multiple endpoints.
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.5 (Surface Tension)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 115 (Surface Tension of Aqueous Solutions)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- ring method
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No. of test material: CBI
- Expiration date of the lot/batch: 02 February 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature, in the dark - Key result
- Surface tension:
- 56.8 mN/m
- Temp.:
- 21 °C
- Conc.:
- 0.1 g/L
- Conclusions:
- The surface tension, of solutions prepared at nominally 0.1 g/L of test item in water and diluted to 90% saturation, has been determined to be 56.8 mN/m at 21.0 ± 0.5 °C. The test item was considered to be surface-active.
- Executive summary:
Surface Tension was determined to be 56.8 ± 0.5 mN/m at 21.0 ± 0.5 °C (for solutions prepared at nominally 0.1 g/L of test item in water and diluted to 90 % saturation), using a ring method, designed to be compatible with Method A5 Surface Tension of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 115 of the OECD Guidelines for Testing of Chemicals, 27 July 1995. The test item was considered to be surface-active.
Sample 1:
Time (mins) | Reading (mN/m) |
Temperature (°C) |
71 | 56.0 | 20.8 |
109 | 56 | 20.8 |
122 | 56.5 | 21.0 |
133 | 56.5 | 21.0 |
143 | 56.5 | 21.2 |
Sample 2:
Time (mins) | Reading (mN/m) | Temperature (°C) |
182 | 57.0 | 21.2 |
240 | 57.0 | 21.4 |
250 | 57.0 | 21.4 |
265 | 57.5 | 21.4 |
275 | 57.5 | 21.4 |
Data source
Reference
- Reference Type:
- study report
- Title:
- Unnamed
- Year:
- 2 016
- Report date:
- 2016
Materials and methods
Test guidelineopen allclose all
- Qualifier:
- according to guideline
- Guideline:
- EU Method A.6 (Water Solubility)
- Deviations:
- no
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 105 (Water Solubility)
- Deviations:
- no
- GLP compliance:
- yes (incl. QA statement)
- Type of method:
- flask method
Test material
- Reference substance name:
- Fatty acids, lanolin, Me esters
- EC Number:
- 284-974-4
- EC Name:
- Fatty acids, lanolin, Me esters
- Cas Number:
- 85005-41-0
- Molecular formula:
- C20H40O2
- IUPAC Name:
- Fatty acids, lanolin, Me esters
- Test material form:
- liquid
Constituent 1
- Specific details on test material used for the study:
- SOURCE OF TEST MATERIAL
- Source and lot/batch No. of test material: CBI
- Expiration date of the lot/batch: 02 February 2018
STABILITY AND STORAGE CONDITIONS OF TEST MATERIAL
- Storage condition of test material: Room temperature, in the dark
Results and discussion
Water solubility
- Key result
- Water solubility:
- < 0.032 g/L
- Conc. based on:
- test mat.
- Loading of aqueous phase:
- 0.1 g/L
- Incubation duration:
- 24 h
- Temp.:
- 20 °C
- pH:
- 5.8
- Details on results:
- The preliminary estimate of water solubility at 20.0 ± 0.5 °C was determined to be less than 4.92 x 10^-2 g/L. The solution had a pH of 5.1.
The mean total peak areas relating to the standard and sample solutions are shown in the following tables two tables:
Any other information on results incl. tables
Samples 1 to 3:
Solution | Mean Total Peak Area |
Standard 1.06 mg/L | 2.567E+07 |
Standard 2.66 mg/L | 5.217E+07 |
Standard 5.29 mg/L | 9.872E+07 |
Standard 7.97 mg/L | 1.457E+08 |
Standard 10.6 mg/L | 1.944E+08 |
Standard 13.3 mg/L | 2.465E+08 |
Standard 15.9 mg/L | 2.772E+08 |
Blank | 4.464E+06 |
Sample 1A | 1.531E+08 |
Sample 1B | 1.510E+08 |
Sample 2A | 1.606E+08 |
Sample 2B | 1.531E+08 |
Sample 3A | 2.830E+08 |
Sample 3B | 2.926E+08 |
Sample 4:
Solution | Mean Total Peak Area |
Standard 1.04 mg/L | 3.833E+07 |
Standard 2.59 mg/L | 8.709E+07 |
Standard 5.38 mg/L | 1.701E+08 |
Standard 7.77 mg/L | 2.452E+08 |
Standard 10.4 mg/L | 3.440E+08 |
Standard 13.0 mg/L | 4.069E+08 |
Standard 15.5 mg/L | 4.595E+08 |
Blank | 3.479E+06 |
Sample 4A | 6.061E+08 |
Sample 4B | 5.952E+08 |
Applicant's summary and conclusion
- Conclusions:
- The water solubility of the test item has been determined to be less than 3.22 x 10^-2 g/L at 20.0 ± 0.5 °C.
- Executive summary:
Water Solubility was determined to be less than 3.22 x 10^-2 g/L of solution at 20.0 ± 0.5 °C, using the flask method, designed to be compatible with Method A.6 Water Solubility of Commission Regulation (EC) No 440/2008 of 30 May 2008 and Method 105 of the OECD Guidelines for Testing of Chemicals, 27 July 1995.
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